RU2743343C2 - Имидазолонилхинолины и их применение в качестве ингибиторов киназы атм - Google Patents

Имидазолонилхинолины и их применение в качестве ингибиторов киназы атм Download PDF

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RU2743343C2
RU2743343C2 RU2017138100A RU2017138100A RU2743343C2 RU 2743343 C2 RU2743343 C2 RU 2743343C2 RU 2017138100 A RU2017138100 A RU 2017138100A RU 2017138100 A RU2017138100 A RU 2017138100A RU 2743343 C2 RU2743343 C2 RU 2743343C2
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methyl
pyrazol
fluoro
het
methoxy
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RU2017138100A
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RU2017138100A3 (zh
RU2017138100A (ru
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Томас ФУКС
Кай Шиманн
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Мерк Патент Гмбх
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/4353Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4375Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having nitrogen as a ring heteroatom, e.g. quinolizines, naphthyridines, berberine, vincamine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/506Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2300/00Mixtures or combinations of active ingredients, wherein at least one active ingredient is fully defined in groups A61K31/00 - A61K41/00

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  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
RU2017138100A 2015-04-02 2016-03-31 Имидазолонилхинолины и их применение в качестве ингибиторов киназы атм RU2743343C2 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
EP15000968.6 2015-04-02
EP15000968 2015-04-02
PCT/EP2016/000542 WO2016155884A1 (de) 2015-04-02 2016-03-31 Imidazolonylchinoline und deren verwendung als atm kinase inhibitoren

Publications (3)

Publication Number Publication Date
RU2017138100A RU2017138100A (ru) 2019-05-08
RU2017138100A3 RU2017138100A3 (zh) 2019-10-04
RU2743343C2 true RU2743343C2 (ru) 2021-02-17

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RU2017138100A RU2743343C2 (ru) 2015-04-02 2016-03-31 Имидазолонилхинолины и их применение в качестве ингибиторов киназы атм

Country Status (24)

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US (5) US10457677B2 (zh)
EP (3) EP3277681B1 (zh)
JP (2) JP6791873B2 (zh)
KR (2) KR20240044525A (zh)
CN (3) CN111747952A (zh)
AU (3) AU2016239270B2 (zh)
BR (1) BR122019005502B1 (zh)
CA (1) CA2981365A1 (zh)
DK (2) DK3560924T3 (zh)
ES (3) ES2946507T3 (zh)
HR (2) HRP20191396T1 (zh)
HU (2) HUE054745T2 (zh)
IL (3) IL254714B (zh)
LT (2) LT3277681T (zh)
MX (2) MX2020011558A (zh)
PL (2) PL3277681T3 (zh)
PT (2) PT3277681T (zh)
RS (2) RS62082B1 (zh)
RU (1) RU2743343C2 (zh)
SG (2) SG11201708065QA (zh)
SI (2) SI3277681T1 (zh)
TR (1) TR201911244T4 (zh)
WO (1) WO2016155884A1 (zh)
ZA (1) ZA201707423B (zh)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016155884A1 (de) * 2015-04-02 2016-10-06 Merck Patent Gmbh Imidazolonylchinoline und deren verwendung als atm kinase inhibitoren
GB201516504D0 (en) 2015-09-17 2015-11-04 Astrazeneca Ab Imadazo(4,5-c)quinolin-2-one Compounds and their use in treating cancer
GB201519406D0 (en) * 2015-11-03 2015-12-16 Astrazeneca Ab Imidazo[4,5-c]quinolin-2-one compounds and their use in treating cancer
WO2018153365A1 (zh) * 2017-02-27 2018-08-30 上海瑛派药业有限公司 取代的稠合杂芳三环化合物作为激酶抑制剂及其应用
JOP20190209A1 (ar) * 2017-03-16 2019-09-12 Astrazeneca Ab مركبات إيميدازو [ 4، 5-c ] كينولين-2-أون ديوترومية واستخدامها في علاج السرطان
AU2019206623A1 (en) 2018-01-12 2020-07-16 Prolynx Llc Synergistic cancer treatment
CA3093499A1 (en) * 2018-03-14 2019-09-19 Merck Patent Gmbh Compounds and uses thereof to treat tumors in a subject
ES2965494T3 (es) 2018-04-12 2024-04-15 Bayer Ag Derivados de N-(ciclopropilmetil)-5-(metilsulfonil)-n-{1-[1-(pirimidin-2-il)-1H-1,2,4-triazol-5-il]etil}benzamida y los correspondientes derivados de piridina-carboxamida como plaguicidas
WO2019201283A1 (en) * 2018-04-20 2019-10-24 Xrad Therapeutics, Inc. Dual atm and dna-pk inhibitors for use in anti-tumor therapy
CN110386932A (zh) * 2018-04-20 2019-10-29 艾科思莱德制药公司 用于抗肿瘤疗法中的双重atm和dna-pk抑制剂
GB201814487D0 (en) * 2018-09-06 2018-10-24 Cycle Pharmaceuticals Ltd Cancer
CN109045042A (zh) * 2018-09-21 2018-12-21 上海交通大学医学院附属上海儿童医学中心 Atm抑制剂在制备抑制急性淋巴细胞性白血病复发的药物中的应用
JP6997358B2 (ja) * 2018-09-30 2022-01-17 メッドシャイン ディスカバリー インコーポレイテッド キノリノピロリジン-2-オン系誘導化合物及びその使用
KR20210143263A (ko) * 2019-03-27 2021-11-26 메르크 파텐트 게엠베하 이미다졸로닐퀴놀린 화합물 및 그의 치료적 용도
BR112022001067A2 (pt) * 2019-07-30 2022-05-24 Xrad Therapeutics Inc Inibidores duplos de atm e dna-pk para uso em terapia antitumoral
JP2023501971A (ja) 2019-11-01 2023-01-20 アレス トレーディング ソシエテ アノニム 癌の治療のための、放射線療法と共に用いるPD-1、TGFβ、及びATMの組み合わせ阻害
EP4069366A1 (en) 2019-12-04 2022-10-12 CHDI Foundation, Inc. Atm kinase inhibitors and compositions and methods of use thereof
WO2021139814A1 (zh) * 2020-01-09 2021-07-15 南京明德新药研发有限公司 喹啉并咪唑类化合物及其应用
WO2021197339A1 (zh) * 2020-03-30 2021-10-07 南京明德新药研发有限公司 作为atm抑制剂的喹啉并吡咯烷-2-酮类化合物的晶型及其应用
CN115916203A (zh) * 2020-06-18 2023-04-04 默克专利股份公司 用于治疗病毒感染的化合物
CN116194109A (zh) 2020-06-24 2023-05-30 阿斯利康(英国)有限公司 抗体-药物缀合物和atm抑制剂的组合
CA3190226A1 (en) 2020-09-18 2022-03-24 Merck Patent Gmbh Pharmaceutical preparation
EP4142710B1 (en) * 2020-09-21 2024-01-31 Wei Zhong Substituted 1-(3,3-difluoropiperidin-4-yl)-imidazo[4,5-c] quinolin-2-one compounds with blood-brain barrier penetrable capability
EP3992191A1 (en) 2020-11-03 2022-05-04 Deutsches Krebsforschungszentrum Imidazo[4,5-c]quinoline compounds and their use as atm kinase inhibitors
CN115232122B (zh) * 2021-04-23 2024-05-31 石药集团中奇制药技术(石家庄)有限公司 炔类化合物及其制备和应用
CN115716829B (zh) * 2022-11-13 2024-05-31 药康众拓(江苏)医药科技有限公司 一种喹啉并咪唑酮联氘代吡唑类化合物及其应用
WO2024112796A1 (en) * 2022-11-23 2024-05-30 Forward Therapeutics, Inc. MODULATORS OF TNF-α ACTIVITY

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2007139008A (ru) * 2005-03-21 2009-04-27 Феррер Интернасионал, С.А. (Es) 1-ЗАМЕЩЕННЫЕ СОЕДИНЕНИЯ 1Н-ИМИДАЗО[4,5-c]ХИНОЛИН-4-АМИНА И СПОСОБ ИХ ПОЛУЧЕНИЯ
WO2010139731A1 (en) * 2009-06-04 2010-12-09 Novartis Ag 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES
WO2011054846A1 (en) * 2009-11-05 2011-05-12 Glaxosmithkline Llc Imidazo [4, 5-c] quinoline derivates as bromodomain inhibitors
RU2010153582A (ru) * 2008-06-10 2012-07-20 Эбботт Лэборетриз (Us) Новые трициклические соединения

Family Cites Families (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0211649D0 (en) 2002-05-21 2002-07-03 Novartis Ag Organic compounds
GB0510390D0 (en) 2005-05-20 2005-06-29 Novartis Ag Organic compounds
CN104758288A (zh) 2007-02-20 2015-07-08 诺华股份有限公司 作为脂质激酶和mTOR双重抑制剂的咪唑并喹啉类
MX338088B (es) 2008-03-26 2016-04-01 Novartis Ag Imidazoquinolinas y derivados de pirimidina como moduladores potentes de los procesos angiogenicos impulsados por el factor de crecimiento endotelial vascular (vegf).
EP3023097A1 (en) 2008-10-01 2016-05-25 Novartis AG Smoothened antagonism for the treatment of hedgehog pathway-related disorders
EP2438063A1 (en) 2009-06-04 2012-04-11 Novartis AG 1h-imidazo[4,5-c]quinolinone compounds, useful for the treatment of proliferative diseases
JP2013522249A (ja) * 2010-03-16 2013-06-13 メルク パテント ゲゼルシャフト ミット ベシュレンクテル ハフツング モルホリニルキナゾリン
SG186855A1 (en) * 2010-06-28 2013-02-28 Merck Patent Gmbh 2,4- diaryl - substituted [1,8] naphthyridines as kinase inhibitors for use against cancer
CN102372711B (zh) 2010-08-18 2014-09-17 山东轩竹医药科技有限公司 咪唑并喹啉类PI3K和mTOR双重抑制剂
DE102010035744A1 (de) 2010-08-28 2012-03-01 Merck Patent Gmbh Imidazolonylchinoline
CN102399218A (zh) 2010-09-16 2012-04-04 和记黄埔医药(上海)有限公司 一类并合三杂环及其作为pi3k抑制剂的用途
US20130245061A1 (en) 2010-12-03 2013-09-19 Novartis Ag Pharmaceutical compositions
CN103012398B (zh) 2011-09-19 2015-10-14 上海恒瑞医药有限公司 咪唑并喹啉类衍生物及其可药用盐、其制备方法及其在医药上的应用
WO2013154778A1 (en) 2012-04-11 2013-10-17 Dana-Farber Cancer Institute, Inc. Host targeted inhibitors of dengue virus and other viruses
CA2872541A1 (en) 2012-06-06 2013-12-12 Novartis Ag Combination of a 17 -alpha -hydroxylase (c17, 20 - lyase) inhibitor and a specific pi-3k inhibitor for treating a tumor disease
NO2714752T3 (zh) 2014-05-08 2018-04-21
WO2016155884A1 (de) 2015-04-02 2016-10-06 Merck Patent Gmbh Imidazolonylchinoline und deren verwendung als atm kinase inhibitoren

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU2007139008A (ru) * 2005-03-21 2009-04-27 Феррер Интернасионал, С.А. (Es) 1-ЗАМЕЩЕННЫЕ СОЕДИНЕНИЯ 1Н-ИМИДАЗО[4,5-c]ХИНОЛИН-4-АМИНА И СПОСОБ ИХ ПОЛУЧЕНИЯ
RU2010153582A (ru) * 2008-06-10 2012-07-20 Эбботт Лэборетриз (Us) Новые трициклические соединения
WO2010139731A1 (en) * 2009-06-04 2010-12-09 Novartis Ag 1H-IMIDAZO[4,5-c]QUINOLINONE DERIVATIVES
WO2011054846A1 (en) * 2009-11-05 2011-05-12 Glaxosmithkline Llc Imidazo [4, 5-c] quinoline derivates as bromodomain inhibitors

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CN111689963A (zh) 2020-09-22
HRP20191396T1 (hr) 2019-11-01
US20230203034A1 (en) 2023-06-29
JP6791873B2 (ja) 2020-11-25
IL254714A0 (en) 2017-11-30
US10975075B2 (en) 2021-04-13
US11608338B2 (en) 2023-03-21
MX2020011558A (es) 2022-03-09
SG10202002181UA (en) 2020-05-28
ZA201707423B (en) 2021-05-26
EP3277681A1 (de) 2018-02-07
BR112017020941A2 (pt) 2018-07-10
US10457677B2 (en) 2019-10-29
JP2018510191A (ja) 2018-04-12
SI3277681T1 (sl) 2019-09-30
IL282584A (en) 2021-06-30
US20210198257A1 (en) 2021-07-01
KR20170132323A (ko) 2017-12-01
KR102652052B1 (ko) 2024-03-27
BR122019005502B1 (pt) 2024-02-27
CN111747952A (zh) 2020-10-09
RU2017138100A3 (zh) 2019-10-04
MX2017012613A (es) 2018-01-24
US10745399B2 (en) 2020-08-18
EP3560924A1 (de) 2019-10-30
RS62082B1 (sr) 2021-08-31
EP3560924B1 (de) 2021-03-31
TR201911244T4 (tr) 2019-08-21
IL282584B (en) 2021-12-01
KR20240044525A (ko) 2024-04-04
HUE054745T2 (hu) 2021-09-28
HUE045477T2 (hu) 2019-12-30
HRP20210981T1 (hr) 2021-09-17
CA2981365A1 (en) 2016-10-06
JP2021046403A (ja) 2021-03-25
AU2022256215A1 (en) 2022-11-24
DK3560924T3 (da) 2021-06-28
US20190211013A1 (en) 2019-07-11
RS59139B1 (sr) 2019-09-30
RU2017138100A (ru) 2019-05-08
SI3560924T1 (sl) 2021-08-31
LT3277681T (lt) 2019-08-12
IL271494B (en) 2021-05-31
PT3277681T (pt) 2019-08-20
EP3868761B1 (de) 2023-03-01
DK3277681T3 (da) 2019-07-29
AU2016239270A1 (en) 2017-11-16
SG11201708065QA (en) 2017-10-30
ES2741853T3 (es) 2020-02-12
WO2016155884A1 (de) 2016-10-06
AU2020204241B2 (en) 2022-11-17
LT3560924T (lt) 2021-08-25
EP3868761A1 (de) 2021-08-25
US20180072715A1 (en) 2018-03-15
AU2020204241A1 (en) 2020-07-16
ES2946507T3 (es) 2023-07-20
CN107889488A (zh) 2018-04-06
JP7111790B2 (ja) 2022-08-02
PL3277681T3 (pl) 2019-10-31
EP3277681B1 (de) 2019-05-08
PL3560924T3 (pl) 2021-10-11
PT3560924T (pt) 2021-07-02
AU2016239270B2 (en) 2020-03-26
IL271494A (en) 2020-02-27
ES2880626T3 (es) 2021-11-25
IL254714B (en) 2020-01-30
CN107889488B (zh) 2020-08-11
US20200325137A1 (en) 2020-10-15

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